A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845206



Internal ID22028849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38055419..38055419hg38UCSC Ensembl
chr13:38629556..38629556hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248930
Supporting Variants
Samples
Known GenesLINC00571
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845206
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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